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DOID:0111324 - juvenile absence epilepsy 1
Disease Ontology Definition:A juvenile absence epilepsy that has_material_basis_in heterozygous mutation in EFHC1 on 6p12.2.
Synonyms: EJA1, JAE1,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
juvenile absence epilepsy (is_a)